Canonical Allele Identifier: CA716979524

Gene: IDH2

Linked Data

• dbSNP Id: rs1170349478
• MyVariant Identifiers: chr15:g.90631534_90631535del (hg19) ; chr15:g.90088302_90088303del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088305_90088306del , CM000677.2:g.90088305_90088306del	GRCh38
NC_000015.9:g.90631537_90631538del , CM000677.1:g.90631537_90631538del	GRCh37
NC_000015.8:g.88432541_88432542del	NCBI36
NG_023302.1:g.19174_19175del , LRG_611:g.19174_19175del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.678+56_678+57del MANE Select	ENSP00000331897.4:n.678+56_678+57del
ENST00000330062.7:c.678+56_678+57del	ENSP00000331897.3:n.678+56_678+57del
ENST00000540499.2:c.522+56_522+57del	ENSP00000446147.2:n.522+56_522+57del
ENST00000559482.5:c.351+56_351+57del	ENSP00000453016.1:n.351+56_351+57del
ENST00000560061.1:c.*303+56_*303+57del	ENSP00000453254.1:n.*303+56_*303+57del
NM_001289910.1:c.522+56_522+57del , LRG_611t1:c.522+56_522+57del	NP_001276839.1:n.522+56_522+57del
NM_001290114.1:c.288+56_288+57del	NP_001277043.1:n.288+56_288+57del
NM_002168.3:c.678+56_678+57del , LRG_611t2:c.678+56_678+57del	NP_002159.2:n.678+56_678+57del
NM_001290114.2:c.288+56_288+57del	NP_001277043.1:n.288+56_288+57del
NM_002168.4:c.678+56_678+57del MANE Select	NP_002159.2:n.678+56_678+57del